| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2444 | missense_variant | HAND2 | NM_021973.3:c.194G>T | G/T | non-isolated CHD: VSD, PS |
| S2445 | missense_variant | HAND2 | NM_021973.3:c.194G>T | G/T | non-isolated CHD: VSD, PS |
| S2448 | missense_variant | HAND2 | NM_021973.3:c.194G>T | G/T | non-isolated CHD: VSD, PS |